Canonical Allele Identifier: CA375682188

Gene: ABO

Linked Data

• dbSNP Id: rs1834555164
• MyVariant Identifiers: chr9:g.136130995C>T (hg19) ; chr9:g.133255608C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255608C>T , CM000671.2:g.133255608C>T	GRCh38
NC_000009.11:g.136130995C>T , CM000671.1:g.136130995C>T	GRCh37
NC_000009.10:g.135120816C>T	NCBI36
NG_006669.1:g.22060G>A
NG_006669.2:g.24608G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1152G>A
ENST00000647353.1:n.54-4456G>A
ENST00000679909.1:c.28+19554G>A	ENSP00000506089.1:n.28+19554G>A
ENST00000453660.3:n.1134G>A
ENST00000538324.2:c.1116G>A	ENSP00000483018.1:p.Trp372Ter
ENST00000611156.4:c.*58G>A	ENSP00000483265.1:n.*58G>A
NM_020469.2:c.*58G>A	NP_065202.2:n.*58G>A
NM_020469.3:c.*58G>A	NP_065202.2:n.*58G>A